JP4471262B2 - 置換イソキサゾールアルキルアミン誘導体及び農園芸用殺菌剤 - Google Patents
置換イソキサゾールアルキルアミン誘導体及び農園芸用殺菌剤 Download PDFInfo
- Publication number
- JP4471262B2 JP4471262B2 JP2003572970A JP2003572970A JP4471262B2 JP 4471262 B2 JP4471262 B2 JP 4471262B2 JP 2003572970 A JP2003572970 A JP 2003572970A JP 2003572970 A JP2003572970 A JP 2003572970A JP 4471262 B2 JP4471262 B2 JP 4471262B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- methyl
- compound
- isoxazolyl
- preparation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 0 CC*C(C1C)(C1(Cl)Cl)C(NC(C)c1cc(-c2ccccc2)n[o]1)=O Chemical compound CC*C(C1C)(C1(Cl)Cl)C(NC(C)c1cc(-c2ccccc2)n[o]1)=O 0.000 description 5
- BOAJURMWMOGBPK-WSDLNYQXSA-N Cc(cc1)ccc1C(NCc1cc(-c2ccc(/C=N/OC)cc2)n[o]1)=O Chemical compound Cc(cc1)ccc1C(NCc1cc(-c2ccc(/C=N/OC)cc2)n[o]1)=O BOAJURMWMOGBPK-WSDLNYQXSA-N 0.000 description 2
- RZFYSUIBQYLHKC-UHFFFAOYSA-N C=[Br]c(cc1)ccc1-c1n[o]c(CNC(c2ccccc2)=O)c1 Chemical compound C=[Br]c(cc1)ccc1-c1n[o]c(CNC(c2ccccc2)=O)c1 RZFYSUIBQYLHKC-UHFFFAOYSA-N 0.000 description 1
- YVEKCOGOXGDPSA-UHFFFAOYSA-N CC(C)Cc1n[o]c(CNC(Oc2ccccc2)=O)c1 Chemical compound CC(C)Cc1n[o]c(CNC(Oc2ccccc2)=O)c1 YVEKCOGOXGDPSA-UHFFFAOYSA-N 0.000 description 1
- DSXCSIUIGPKUFQ-UHFFFAOYSA-N CC(C)Cc1n[o]c(CNC(c(cc2)ccc2Cl)=O)c1 Chemical compound CC(C)Cc1n[o]c(CNC(c(cc2)ccc2Cl)=O)c1 DSXCSIUIGPKUFQ-UHFFFAOYSA-N 0.000 description 1
- VLTGLNOAUDXWPB-UHFFFAOYSA-N CC(C)Cc1n[o]c(CNC(c2cc3ccccc3cc2)=O)c1 Chemical compound CC(C)Cc1n[o]c(CNC(c2cc3ccccc3cc2)=O)c1 VLTGLNOAUDXWPB-UHFFFAOYSA-N 0.000 description 1
- VBNOERFDYOTMJA-UHFFFAOYSA-N CC(C1(C)C(NCc2cc(-c3ccccc3)n[o]2)=O)C1(Cl)Cl Chemical compound CC(C1(C)C(NCc2cc(-c3ccccc3)n[o]2)=O)C1(Cl)Cl VBNOERFDYOTMJA-UHFFFAOYSA-N 0.000 description 1
- LJJNEBNFVXLVEM-UHFFFAOYSA-N CCCCc1n[o]c(CNC(c(cc2)ccc2OC)=O)c1 Chemical compound CCCCc1n[o]c(CNC(c(cc2)ccc2OC)=O)c1 LJJNEBNFVXLVEM-UHFFFAOYSA-N 0.000 description 1
- SQNMHZPURDLMGB-UHFFFAOYSA-N CCCc(cc1)ccc1C(NCc1cc(CCl)n[o]1)=O Chemical compound CCCc(cc1)ccc1C(NCc1cc(CCl)n[o]1)=O SQNMHZPURDLMGB-UHFFFAOYSA-N 0.000 description 1
- MRZPSROMNZJLHH-UHFFFAOYSA-N CN(C(NCc1cc(-c2ccccc2)n[o]1)=O)c1ccccc1 Chemical compound CN(C(NCc1cc(-c2ccccc2)n[o]1)=O)c1ccccc1 MRZPSROMNZJLHH-UHFFFAOYSA-N 0.000 description 1
- HJABNDNDPAFBJE-UHFFFAOYSA-N CNC(c1n[o]c(CNC(NC2CCCCC2)=O)c1)=O Chemical compound CNC(c1n[o]c(CNC(NC2CCCCC2)=O)c1)=O HJABNDNDPAFBJE-UHFFFAOYSA-N 0.000 description 1
- FJUADDDIFMFBFR-UHFFFAOYSA-N COC(c1cccc(OCc2n[o]c(CNC(c(cc3)ccc3OC)=O)c2)c1)=O Chemical compound COC(c1cccc(OCc2n[o]c(CNC(c(cc3)ccc3OC)=O)c2)c1)=O FJUADDDIFMFBFR-UHFFFAOYSA-N 0.000 description 1
- YSVMCWGFZVMZJV-UHFFFAOYSA-N COc(cc1)ccc1C(NCc1cc(C(Nc(cc2)ccc2F)=O)n[o]1)=O Chemical compound COc(cc1)ccc1C(NCc1cc(C(Nc(cc2)ccc2F)=O)n[o]1)=O YSVMCWGFZVMZJV-UHFFFAOYSA-N 0.000 description 1
- DOWPADDFANWJLD-UHFFFAOYSA-N COc(cc1)ccc1C(NCc1cc(C(Nc(cccc2)c2C#N)=O)n[o]1)=O Chemical compound COc(cc1)ccc1C(NCc1cc(C(Nc(cccc2)c2C#N)=O)n[o]1)=O DOWPADDFANWJLD-UHFFFAOYSA-N 0.000 description 1
- TVDAUPPDHQRIFJ-FSJBWODESA-N COc(cc1)ccc1C(NCc1cc(CO[IH]/N=C/c2ccccc2)n[o]1)=O Chemical compound COc(cc1)ccc1C(NCc1cc(CO[IH]/N=C/c2ccccc2)n[o]1)=O TVDAUPPDHQRIFJ-FSJBWODESA-N 0.000 description 1
- HASQDFAFNPEPHP-UHFFFAOYSA-N COc(cc1)ccc1C(NCc1cc(COc(cccc2)c2OC)n[o]1)=O Chemical compound COc(cc1)ccc1C(NCc1cc(COc(cccc2)c2OC)n[o]1)=O HASQDFAFNPEPHP-UHFFFAOYSA-N 0.000 description 1
- DQPGHJIKCSXNPE-UHFFFAOYSA-N COc(cc1)ccc1C(NCc1cc(COc2ccccn2)n[o]1)=O Chemical compound COc(cc1)ccc1C(NCc1cc(COc2ccccn2)n[o]1)=O DQPGHJIKCSXNPE-UHFFFAOYSA-N 0.000 description 1
- CHLWZQJZUQDANU-UHFFFAOYSA-N COc1ccc(C(NCc2cc(COc(cc3)ccc3-[n]3cncc3)n[o]2)O)cc1 Chemical compound COc1ccc(C(NCc2cc(COc(cc3)ccc3-[n]3cncc3)n[o]2)O)cc1 CHLWZQJZUQDANU-UHFFFAOYSA-N 0.000 description 1
- BLGHWHAFZQFTCT-UHFFFAOYSA-N CS(C(CC1)=CCC1C(NCC1c2c1c(CCl)n[o]2)=O)(=O)=O Chemical compound CS(C(CC1)=CCC1C(NCC1c2c1c(CCl)n[o]2)=O)(=O)=O BLGHWHAFZQFTCT-UHFFFAOYSA-N 0.000 description 1
- XCDSVJSQWOOXMM-UHFFFAOYSA-N Cc(cc1)ccc1C(NCc1cc(-c(cc2)ccc2F)n[o]1)=O Chemical compound Cc(cc1)ccc1C(NCc1cc(-c(cc2)ccc2F)n[o]1)=O XCDSVJSQWOOXMM-UHFFFAOYSA-N 0.000 description 1
- PWUZEGIVFLUSTI-UHFFFAOYSA-N Cc(cc1)ccc1C(NCc1cc(-c(ccc(OC)c2)c2F)n[o]1)=O Chemical compound Cc(cc1)ccc1C(NCc1cc(-c(ccc(OC)c2)c2F)n[o]1)=O PWUZEGIVFLUSTI-UHFFFAOYSA-N 0.000 description 1
- NTABUAASHVBFKZ-UHFFFAOYSA-N Cc(cc1)ccc1C(NCc1cc(-c2ncccc2)n[o]1)=O Chemical compound Cc(cc1)ccc1C(NCc1cc(-c2ncccc2)n[o]1)=O NTABUAASHVBFKZ-UHFFFAOYSA-N 0.000 description 1
- AHDWTXVIAFLIMT-VOTSOKGWSA-N O=C(/C=C/c1ccccc1)NCc1cc(CCl)n[o]1 Chemical compound O=C(/C=C/c1ccccc1)NCc1cc(CCl)n[o]1 AHDWTXVIAFLIMT-VOTSOKGWSA-N 0.000 description 1
- CZEIOVIIRLLPKH-UHFFFAOYSA-N O=C(NC1c2c1c(-c1ccccc1)n[o]2)Nc(cc1)ccc1Oc1ccccc1 Chemical compound O=C(NC1c2c1c(-c1ccccc1)n[o]2)Nc(cc1)ccc1Oc1ccccc1 CZEIOVIIRLLPKH-UHFFFAOYSA-N 0.000 description 1
- GSHFVAMZAGMOQC-UHFFFAOYSA-N O=C(NCc1cc(-c2ccccc2)n[o]1)Nc(cc1)ccc1OC1=CC=CCC1 Chemical compound O=C(NCc1cc(-c2ccccc2)n[o]1)Nc(cc1)ccc1OC1=CC=CCC1 GSHFVAMZAGMOQC-UHFFFAOYSA-N 0.000 description 1
- CDGZPHQHRCHCEX-UHFFFAOYSA-N O=C(NCc1cc(-c2ccccc2)n[o]1)Nc1ccccc1 Chemical compound O=C(NCc1cc(-c2ccccc2)n[o]1)Nc1ccccc1 CDGZPHQHRCHCEX-UHFFFAOYSA-N 0.000 description 1
- VHSRKUKZHOYCBY-UHFFFAOYSA-N O=C(NCc1cc(-c2ccccc2Cl)n[o]1)Oc1ccccc1 Chemical compound O=C(NCc1cc(-c2ccccc2Cl)n[o]1)Oc1ccccc1 VHSRKUKZHOYCBY-UHFFFAOYSA-N 0.000 description 1
- BEIHVNMLEAGQIE-UHFFFAOYSA-N O=C(NCc1cc(Cc2ccccc2)n[o]1)NC1CCCC1 Chemical compound O=C(NCc1cc(Cc2ccccc2)n[o]1)NC1CCCC1 BEIHVNMLEAGQIE-UHFFFAOYSA-N 0.000 description 1
- HKSNEMSLKBXRFE-UHFFFAOYSA-N O=C(c(c(Cl)ccc1)c1Cl)NCc1cc(CCl)n[o]1 Chemical compound O=C(c(c(Cl)ccc1)c1Cl)NCc1cc(CCl)n[o]1 HKSNEMSLKBXRFE-UHFFFAOYSA-N 0.000 description 1
- CEEXGNDLFTXYCL-UHFFFAOYSA-N O=C(c1cc(F)ccc1)NCc1cc(CCl)n[o]1 Chemical compound O=C(c1cc(F)ccc1)NCc1cc(CCl)n[o]1 CEEXGNDLFTXYCL-UHFFFAOYSA-N 0.000 description 1
- PFHZWTANTUJNJI-UHFFFAOYSA-N O=C(c1cccc(Cl)c1)NCC1=CC(CCl)NO1 Chemical compound O=C(c1cccc(Cl)c1)NCC1=CC(CCl)NO1 PFHZWTANTUJNJI-UHFFFAOYSA-N 0.000 description 1
- ZPISWDYAKZKLTQ-UHFFFAOYSA-N O=C(c1ccccc1)NCc1cc(-c(cc2)ccc2Cl)n[o]1 Chemical compound O=C(c1ccccc1)NCc1cc(-c(cc2)ccc2Cl)n[o]1 ZPISWDYAKZKLTQ-UHFFFAOYSA-N 0.000 description 1
- KMTANKVYWRXQPH-UHFFFAOYSA-N O=C(c1ccccc1)NCc1cc(-c2ccccc2)n[o]1 Chemical compound O=C(c1ccccc1)NCc1cc(-c2ccccc2)n[o]1 KMTANKVYWRXQPH-UHFFFAOYSA-N 0.000 description 1
- HJAUOKAHXCJMQY-UHFFFAOYSA-N O=C(c1cccnc1)NCc1cc(-c2ccccc2)n[o]1 Chemical compound O=C(c1cccnc1)NCc1cc(-c2ccccc2)n[o]1 HJAUOKAHXCJMQY-UHFFFAOYSA-N 0.000 description 1
- OTHGYSHTOORRKZ-UHFFFAOYSA-N OCc1n[o]c(CNC(NC2CCCCC2)=O)c1 Chemical compound OCc1n[o]c(CNC(NC2CCCCC2)=O)c1 OTHGYSHTOORRKZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/84—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/32—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing >N—CO—N< or >N—CS—N< groups directly attached to a cycloaliphatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002061835 | 2002-03-07 | ||
JP2002061835 | 2002-03-07 | ||
PCT/JP2003/002632 WO2003074501A1 (fr) | 2002-03-07 | 2003-03-06 | Derive d'isoxazole alkylamine substitue et fongicide a usage dans l'agriculture et l'horticulture |
Publications (2)
Publication Number | Publication Date |
---|---|
JPWO2003074501A1 JPWO2003074501A1 (ja) | 2005-06-30 |
JP4471262B2 true JP4471262B2 (ja) | 2010-06-02 |
Family
ID=27784871
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2003572970A Expired - Lifetime JP4471262B2 (ja) | 2002-03-07 | 2003-03-06 | 置換イソキサゾールアルキルアミン誘導体及び農園芸用殺菌剤 |
Country Status (5)
Country | Link |
---|---|
US (1) | US20050171358A1 (fr) |
EP (1) | EP1491535A4 (fr) |
JP (1) | JP4471262B2 (fr) |
AU (1) | AU2003221322A1 (fr) |
WO (1) | WO2003074501A1 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2018525440A (ja) * | 2015-07-28 | 2018-09-06 | アダム ミツキェヴィチ ユニバーシティ ファウンデーション | 植物刺激物としての7−カルボキシベンゾ[1,2,3]チアジアゾールアミドの適用 |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MXPA05007513A (es) | 2003-01-14 | 2005-09-21 | Cytokinetics Inc | Compuestos, composiciones y metodos. |
BRPI0512193B8 (pt) | 2004-06-17 | 2021-05-25 | Cytokinetics Inc | composto ou sal farmaceuticamente aceitável, composição farmacêutica, e, uso do composto ou sal |
NZ552187A (en) | 2004-06-18 | 2010-08-27 | Millennium Pharm Inc | Thiophene-2-carboxamide derivatives |
US7696352B2 (en) * | 2004-06-18 | 2010-04-13 | Millennium Pharmaceuticals, Inc. | Factor Xa inhibitors |
US7176222B2 (en) | 2004-07-27 | 2007-02-13 | Cytokinetics, Inc. | Syntheses of ureas |
JP3789465B1 (ja) | 2005-04-28 | 2006-06-21 | 学校法人立教学院 | イソオキサゾール誘導体又はジヒドロイソオキサゾール誘導体の製造方法 |
US7538223B2 (en) | 2005-08-04 | 2009-05-26 | Cytokinetics, Inc. | Compounds, compositions and methods |
TW200808321A (en) | 2005-12-15 | 2008-02-16 | Cytokinetics Inc | Certain chemical entities, compositions and methods |
US7825120B2 (en) | 2005-12-15 | 2010-11-02 | Cytokinetics, Inc. | Certain substituted ((piperazin-1-ylmethyl)benzyl)ureas |
WO2007078815A2 (fr) | 2005-12-16 | 2007-07-12 | Cytokinetics, Inc. | Entites chimiques, compositions et methodes |
EP1962852B1 (fr) | 2005-12-19 | 2017-01-25 | Cytokinetics, Inc. | Composes, compositions et methodes |
CA2651303A1 (fr) | 2006-05-05 | 2007-11-15 | Millennium Pharmaceuticals, Inc. | Inhibiteurs de facteur xa |
WO2008013622A2 (fr) * | 2006-07-27 | 2008-01-31 | E. I. Du Pont De Nemours And Company | Amides azocycliques fongicides |
EP2076511A1 (fr) * | 2006-10-25 | 2009-07-08 | F. Hoffmann-Roche AG | Nouveaux carboxamides heteroaryliques |
US20080293704A1 (en) * | 2007-01-05 | 2008-11-27 | Millennium Pharmaceuticals, Inc. | FACTOR Xa INHIBITORS |
US8058469B2 (en) * | 2008-11-03 | 2011-11-15 | Sabic Innovative Plastics Ip B.V. | Method for making carbamates, ureas and isocyanates |
KR101220182B1 (ko) | 2009-02-25 | 2013-01-11 | 에스케이바이오팜 주식회사 | 치환된 아졸 유도체 화합물, 이를 포함하는 약제학적 조성물 및 이를 이용한 파킨슨씨 병 치료방법 |
CA2784921A1 (fr) * | 2009-12-17 | 2011-07-14 | Millennium Pharmaceuticals, Inc. | Sels et formes cristallines d'inhibiteur de facteur xa |
WO2011075602A1 (fr) * | 2009-12-17 | 2011-06-23 | Millennium Pharmaceuticals, Inc. | Procédés de préparation d'inhibiteurs du facteur xa et de leurs sels |
US8835472B2 (en) * | 2010-09-02 | 2014-09-16 | Boehringer Ingelheim International Gmbh | Compounds, pharmaceutical compositions and uses thereof |
CN111646986B (zh) * | 2017-09-13 | 2022-03-25 | 厦门稀土材料研究所 | 烟酸衍生物及其制备方法与用途 |
CN110066274B (zh) * | 2019-03-19 | 2021-07-23 | 厦门稀土材料研究所 | 吡啶-2-甲酸衍生物及其制备方法与用途 |
CN109942566B (zh) * | 2019-03-19 | 2021-07-23 | 厦门稀土材料研究所 | 异烟酸衍生物及其制备方法和用途 |
AU2021241530A1 (en) * | 2020-03-23 | 2022-10-20 | Praxis Precision Medicines, Inc. | KCNT1 inhibitors and methods of use |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4109002A (en) * | 1976-06-14 | 1978-08-22 | Eli Lilly And Company | Fungicidal 3-phenyl-5-(substituted methyl) isoxaxoles |
DE2842315A1 (de) * | 1978-09-28 | 1980-04-17 | Bayer Ag | N-(1,2-azolyl)alkyl-halogenacetanilide, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide |
US4666502A (en) * | 1982-02-09 | 1987-05-19 | Sandoz Ltd. | Herbicidal N-thienyl-chloroacetamides |
DE3643942A1 (de) * | 1986-12-22 | 1988-06-23 | Bayer Ag | Aminomethylisoxazolidine |
EP0451790A1 (fr) * | 1990-04-12 | 1991-10-16 | Hoechst Aktiengesellschaft | 2-isoxazolines et isoxazoles 3,5-disubstitués, procédé pour leur préparation,médicaments les contenant et leur utilisation |
CA2212836C (fr) * | 1995-02-13 | 2003-08-12 | G.D. Searle & Co. | Isoxazoles substitues utilisables dans le traitement d'inflammations |
EP0761654B1 (fr) * | 1995-08-24 | 2003-06-18 | Basf Aktiengesellschaft | Dérivés d'isoxazole- et d'isothiazole-5-carboxamide, leur préparation et leur utilisation comme herbicides |
FR2773155B1 (fr) * | 1997-12-29 | 2000-01-28 | Rhone Poulenc Agrochimie | Nouveaux composes fongicides |
-
2003
- 2003-03-06 JP JP2003572970A patent/JP4471262B2/ja not_active Expired - Lifetime
- 2003-03-06 EP EP03710257A patent/EP1491535A4/fr not_active Withdrawn
- 2003-03-06 WO PCT/JP2003/002632 patent/WO2003074501A1/fr active Application Filing
- 2003-03-06 AU AU2003221322A patent/AU2003221322A1/en not_active Abandoned
- 2003-03-06 US US10/506,907 patent/US20050171358A1/en not_active Abandoned
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2018525440A (ja) * | 2015-07-28 | 2018-09-06 | アダム ミツキェヴィチ ユニバーシティ ファウンデーション | 植物刺激物としての7−カルボキシベンゾ[1,2,3]チアジアゾールアミドの適用 |
Also Published As
Publication number | Publication date |
---|---|
US20050171358A1 (en) | 2005-08-04 |
JPWO2003074501A1 (ja) | 2005-06-30 |
AU2003221322A1 (en) | 2003-09-16 |
WO2003074501A1 (fr) | 2003-09-12 |
EP1491535A1 (fr) | 2004-12-29 |
EP1491535A4 (fr) | 2009-09-23 |
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